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Analysis of Dystrophin Gene Deletions by Multiplex PCR in Moroccan Patients
Duchenne and Becker muscular dystrophy (DMD and BMD) are X-linked diseases resulting from a defect in the dystrophin gene located on Xp21. DMD is the most frequent neuromuscular disease in humans (1/3500 male newborn). Deletions in the dystrophin gene represent 65% of mutations in DMD/BMD patients....
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
2002
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC161366/ https://www.ncbi.nlm.nih.gov/pubmed/12488581 http://dx.doi.org/10.1155/S1110724302205069 |